salicylic acid [Ligand Id: 4306] activity data from GtoPdb and ChEMBL
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| ChEMBL ligand: CHEMBL424 (2-Hydroxy-benzoic acid, Acnisal, Advanced pain relief callus removers, Advanced pain relief com removers, Bazuka, Clear away wart remover, Compound v, Compound w, Cuplex verruca, Dr. scholl's callus removers, Dr. scholl's corn removers, Dr. scholl's wart remover kit, Duofilm, Duofilm wart remover, Duoplant, Edinburgh, Erytex, FEMA NO. 3985, Freezone, Gppe paint, Ionil, Ionil-plus, Jadit, K-557, Keralyt, Lamivudine impurity, salicylic acid-, Lamivudine related compound salicylic acid, Metanium, Necol, Noxacorn, NSC-180, Occlusal, Phiso-clear, Phytex, Phytocil, Posalfilin, Pyralvex, Salactol, Salatac, Salicylic acid, Salicylic Acid, Salicylic acid rs, Salicylic acid soap, Saligel, Stri-dex, Thwart, Toepedo, Verrugon, Wartex) |
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| DB | Assay description | Assay Type | Standard value | Standard parameter | Original value | Original units | Original parameter | Reference |
|---|---|---|---|---|---|---|---|---|
| Beta amyloid A4 protein in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2487] [UniProtKB: P05067] | ||||||||
| ChEMBL | Inhibitory activity against binding of [125I]IMSB to amyloid beta in brain | B | 5.74 | pKi | >1800 | nM | Ki | J Med Chem (2001) 44: 2270-2275 [PMID:11428920] |
| Carbonic anhydrase 15 in Mouse (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL5973] [UniProtKB: Q99N23] | ||||||||
| ChEMBL | Inhibition of mouse recombinant carbonic anhydrase 15 by stopped-flow CO2 hydrase assay | B | 5.14 | pKi | 7200 | nM | Ki | Bioorg Med Chem Lett (2008) 18: 3593-3596 [PMID:18501600] |
| carbonic anhydrase 1/Carbonic anhydrase I in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL261] [GtoPdb: 2597] [UniProtKB: P00915] | ||||||||
| ChEMBL | Inhibition of human carbonic anhydrase 1 by stopped-flow CO2 hydrase assay | B | 5 | pKi | 9920 | nM | Ki | Bioorg Med Chem Lett (2008) 18: 3593-3596 [PMID:18501600] |
| ChEMBL | Inhibition of human carbonic anhydrase 1 by stopped-flow CO2 hydration assay | B | 5 | pKi | 9900 | nM | Ki | Bioorg Med Chem (2008) 16: 7424-7428 [PMID:18579385] |
| ChEMBL | Inhibition of human carbonic anhydrase 1 incubated for 15 mins prior to testing by stopped flow CO2 hydration assay | B | 5 | pKi | 9900 | nM | Ki | Bioorg Med Chem Lett (2015) 25: 5636-5641 [PMID:26520662] |
| carbonic anhydrase 2/Carbonic anhydrase II in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL205] [GtoPdb: 3092] [UniProtKB: P00918] | ||||||||
| ChEMBL | Inhibition of human carbonic anhydrase 2 by stopped-flow CO2 hydrase assay | B | 5.15 | pKi | 7120 | nM | Ki | Bioorg Med Chem Lett (2008) 18: 3593-3596 [PMID:18501600] |
| ChEMBL | Inhibition of human carbonic anhydrase 2 by stopped-flow CO2 hydration assay | B | 5.15 | pKi | 7100 | nM | Ki | Bioorg Med Chem (2008) 16: 7424-7428 [PMID:18579385] |
| ChEMBL | Inhibition of human carbonic anhydrase 2 incubated for 15 mins prior to testing by stopped flow CO2 hydration assay | B | 5.15 | pKi | 7100 | nM | Ki | Bioorg Med Chem Lett (2015) 25: 5636-5641 [PMID:26520662] |
| carbonic anhydrase 4/Carbonic anhydrase IV in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3729] [GtoPdb: 2599] [UniProtKB: P22748] | ||||||||
| ChEMBL | Inhibition of human carbonic anhydrase 4 by stopped-flow CO2 hydration assay | B | 4.95 | pKi | 11100 | nM | Ki | Bioorg Med Chem (2008) 16: 7424-7428 [PMID:18579385] |
| carbonic anhydrase 9/Carbonic anhydrase IX in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3594] [GtoPdb: 3055] [UniProtKB: Q16790] | ||||||||
| ChEMBL | Inhibition of human carbonic anhydrase 9 catalytic domain by stopped-flow CO2 hydration assay | B | 4.1 | pKi | 78700 | nM | Ki | Bioorg Med Chem (2008) 16: 7424-7428 [PMID:18579385] |
| ChEMBL | Inhibition of human carbonic anhydrase 9 incubated for 15 mins prior to testing by stopped flow CO2 hydration assay | B | 4.1 | pKi | 78700 | nM | Ki | Bioorg Med Chem Lett (2015) 25: 5636-5641 [PMID:26520662] |
| Carbonic anhydrase VI in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3025] [UniProtKB: P23280] | ||||||||
| ChEMBL | Inhibition of human carbonic anhydrase 6 by stopped-flow CO2 hydration assay | B | 4.92 | pKi | 11900 | nM | Ki | Bioorg Med Chem (2008) 16: 7424-7428 [PMID:18579385] |
| carbonic anhydrase 7/Carbonic anhydrase VII in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2326] [GtoPdb: 2749] [UniProtKB: P43166] | ||||||||
| ChEMBL | Inhibition of human carbonic anhydrase 7 by stopped-flow CO2 hydration assay | B | 4.09 | pKi | 82100 | nM | Ki | Bioorg Med Chem (2008) 16: 7424-7428 [PMID:18579385] |
| carbonic anhydrase 12/Carbonic anhydrase XII in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3242] [GtoPdb: 2747] [UniProtKB: O43570] | ||||||||
| ChEMBL | Inhibition of human carbonic anhydrase 12 catalytic domain by stopped-flow CO2 hydration assay | B | 5.06 | pKi | 8800 | nM | Ki | Bioorg Med Chem (2008) 16: 7424-7428 [PMID:18579385] |
| carbonic anhydrase 13/Carbonic anhydrase XIII in Mouse (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2186] [GtoPdb: 2748] [UniProtKB: Q9D6N1] | ||||||||
| ChEMBL | Inhibition of mouse carbonic anhydrase 13 by stopped-flow CO2 hydration assay | B | 4.17 | pKi | 67000 | nM | Ki | Bioorg Med Chem (2008) 16: 7424-7428 [PMID:18579385] |
| carbonic anhydrase 14/Carbonic anhydrase XIV in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3510] [GtoPdb: 2598] [UniProtKB: Q9ULX7] | ||||||||
| ChEMBL | Inhibition of human carbonic anhydrase 14 by stopped-flow CO2 hydration assay | B | 4.3 | pKi | 49800 | nM | Ki | Bioorg Med Chem (2008) 16: 7424-7428 [PMID:18579385] |
| COX-1 /Cyclooxygenase-1 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL221] [GtoPdb: 1375] [UniProtKB: P23219] | ||||||||
| ChEMBL | Inhibition of human COX1 assessed as reduction in PGF2alpha formation using arachidonic acid as substrate incubated for 10 mins by ELISA | B | 4.4 | pIC50 | >40000 | nM | IC50 | Eur J Med Chem (2020) 193: 112217-112217 [PMID:32182488] |
| COX-2 /Cyclooxygenase-2 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL230] [GtoPdb: 1376] [UniProtKB: P35354] | ||||||||
| ChEMBL | Inhibition of human COX2 assessed as reduction in PGF2alpha formation using arachidonic acid as substrate incubated for 10 mins by ELISA | B | 4.4 | pIC50 | >40000 | nM | IC50 | Eur J Med Chem (2020) 193: 112217-112217 [PMID:32182488] |
| High mobility group protein B1 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2311236] [UniProtKB: P09429] | ||||||||
| ChEMBL | Binding affinity to recombinant HMGB1 box A (unknown origin) | B | 6 | pKd | 1000 | nM | Kd | J Med Chem (2018) 61: 5093-5107 [PMID:29268019] |
| ChEMBL | Binding affinity to recombinant HMGB1 box B (unknown origin) | B | 6 | pKd | 1000 | nM | Kd | J Med Chem (2018) 61: 5093-5107 [PMID:29268019] |
| Nicotinate phosphoribosyltransferase in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4523354] [UniProtKB: Q6XQN6] | ||||||||
| ChEMBL | Inhibition of NAPRT (unknown origin) | B | 9.8 | pKi | 0.16 | nM | Ki | WO-2017162840-A1. Sensitization of cancer cells to nampt inhibitors by nicotinic acid phosphoribosyltransferase neutralization (null) |
| OAT6/Solute carrier family 22 member 20 in Mouse (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL5269] [GtoPdb: 1037] [UniProtKB: Q80UJ1] | ||||||||
| ChEMBL | Inhibition of mouse Oat6-mediated [3H]ES uptake in Xenopus oocytes after 1 hr | B | 4.36 | pKi | 44000 | nM | Ki | J Biol Chem (2007) 282: 23841-23853 [PMID:17553798] |
| ChEMBL | Inhibition of mouse Oat6-mediated [3H]ES uptake in Xenopus oocytes after 1 hr | B | 4.36 | pKi | 43651.58 | nM | Ki | J Biol Chem (2007) 282: 23841-23853 [PMID:17553798] |
| Tyrosinase in Agaricus bisporus (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3318] [UniProtKB: O42713] | ||||||||
| ChEMBL | Inhibition of mushroom tyrosinase after 10 mins | B | 4 | pIC50 | 100000 | nM | IC50 | J Med Chem (2011) 54: 591-602 [PMID:21189019] |
| ASIC3 in Human [GtoPdb: 686] [UniProtKB: Q9UHC3] | ||||||||
| GtoPdb | - | - | 3.6 | pIC50 | 260000 | nM | IC50 | J Neurosci (2001) 21: 8026-33 [PMID:11588175] |
ChEMBL data shown on this page come from version 33:
Mendez D, Gaulton A, Bento AP, Chambers J, De Veij M, Félix E, Magariños MP, Mosquera JF, Mutowo P, Nowotka M, Gordillo-Marañón M, Hunter F, Junco L, Mugumbate G, Rodriguez-Lopez M, Atkinson F, Bosc N, Radoux CJ, Segura-Cabrera A, Hersey A, Leach AR. (2019) 'ChEMBL: towards direct deposition of bioassay data' Nucleic Acids Res., 47(D1). DOI: 10.1093/nar/gky1075. [EPMCID:30398643]
Davies M, Nowotka M, Papadatos G, Dedman N, Gaulton A, Atkinson F, Bellis L, Overington JP. (2015) 'ChEMBL web services: streamlining access to drug discovery data and utilities.' Nucleic Acids Res., 43(W1). DOI: 10.1093/nar/gkv352. [EPMCID:25883136]
